The development of thermally conductive rubber nanocomposites for heat management poses a formidable challenge in numerous applications, notably within the realm of tire technology. Notably, rubber materials are characterized by their inherently low thermal conductivity. Consequently, it becomes imperative to incorporate diverse conductive fillers to mitigate the propensity for heat build-up. Multi-walled carbon nanotubes (MWCNTs), as reinforcement agents within the tire tread compounds, have gained considerable attention owing to their extraordinary attributes. The attainment of high-performance rubber nanocomposites hinges significantly on the uniform distribution of MWCNT. This study presents the influence of MWCNTs on the performance of carbon black (CB)-reinforced natural rubber (NR)/styrene butadiene rubber (SBR) tire compounds prepared via high shear melt mixing. Morphological analysis showed a good distribution of MWCNTs in the NR/SBR/CB compound. The vulcanization parameters, such as the maximum and minimum torque, cross-linking density, hardness, abrasion resistance, tensile strength, and Young modulus, exhibited a progressive improvement with the addition of MWCNT. Remarkably, adding MWCNT into CB improved the heat conductivity of the NR/SBR/CB compounds, hence decreasing the heat build-up. A percolation mode was also proposed for the hybrid carbon fillers based on the data obtained.

Thermoplastic vulcanizates (TPVs) are multifunctional materials consisting of two or more phases with solid elastomeric properties at room temperatures and fluid-like properties above their melting point. They are produced through a reactive blending process known as dynamic vulcanization. The most widely produced TPV type is ethylene propylene diene monomer/polypropylene (EPDM/PP), which is the focus of this study. The peroxides are mainly selected to be used in crosslinking of EPDM/PP-based TPV. However, they still have some disadvantages, such as the side reactions resulting in the beta chain scission of the PP phase and undesired disproportionation reactions. To eliminate these disadvantages, coagents are used. In this study, for the first time, the use of vinyl functionalized polyhedral oligomeric silsesquioxane (OV-POSS) nanoparticles was investigated as a potential coagent in EPDM/PP-based TPV production via peroxide-initiated dynamic vulcanization. The properties of the TPVs having POSS were compared with the conventional TPVs containing conventional coagents, such as triallyl cyanurate (TAC). POSS content and EPDM/PP ratio were investigated as the material parameters. Mechanical properties of EPDM/PP TPVs exhibited higher values in the presence of OV-POSS, which resulted from the active participation of OV-POSS into the three-dimensional network structure of EPDM/PP during dynamic vulcanization.

In this study, polyamide 6 (PA6)/thermoplastic elastomer (TPE) blends were prepared to decrease the notch sensitivity of PA6 for automotive applications, and the morphological, rheological, mechanical, and thermal properties of PA6/TPE blends, which are partially miscible or immiscible depending on the TPE ratio, were significantly improved in the existence of polyhedral oligomeric silsesquioxane (POSS) nanoparticles with multiple reactive epoxy groups as compatibilizers. An unstable phase morphology was obtained with the addition of TPE into PA6 without POSS nanoparticles, whereas interfacial interactions between phases in the presence of POSS were enhanced as a result of a significant decrease in the average particle size from 1.39 to 0.41 μm. The complex viscosity value of the 70PA6/30TPE blend, which was 20 kPa/s^-1 at 0.1 rad/s angular frequency, reached 380 kPa/s^-1 with the addition of POSS due to the formation of long chains by the generation of graft and/or block copolymers, which resulted in a 65% increase in Young's modulus value. Most notably, the Izod impact strength of pure PA6, which was 10 kJ/m², increased by 290% with the incorporation of POSS. It was confirmed by FTIR analysis that the reactive multiple epoxy groups of MultEpPOSS and EPPOSS nanoparticles react with the proper groups of PA6 and/or TPE, and also, a partial hydrogen bonding interaction occurs between PA6-TPE from the shifting of N-H and carbonyl peaks. In conclusion, it can be suggested that POSS nanoparticles can serve as highly effective compatibilizers for PA6/TPE blends and have potential commercial applications, especially in the automotive sector.